Clinical Research Associate

🔥 12 hours ago

🇩🇪 Germany – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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Pfizer

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1849

💼 Consulting

📣 Marketing

💊 Pharmaceuticals

💰 Post-IPO Debt on 2023-05

Consulting • Marketing • Pharmaceuticals

Pfizer is a pharmaceutical company that has been at the forefront of scientific innovation for 175 years. The company is dedicated to improving health and well-being at every stage of life by providing access to safe, effective, and affordable medicines and healthcare services. Pfizer focuses on delivering innovative therapies, particularly in the field of cancer treatments, as it continues to progress in transforming the healthcare landscape.

📋 Description

• Manage, monitor, and close out assigned clinical trial sites • Ensure patient safety and the high-quality conduct of clinical trials in accordance with applicable laws and regulations, Good Clinical Practice (GCP), and Pfizer standards • Oversee operational activities from study initiation through ongoing monitoring and close-out, ensuring adherence to quality standards, timelines, and the Study Monitoring Plan • Conduct on-site or remote monitoring, depending on study requirements • Serve as the primary point of contact for assigned clinical trial sites throughout study conduct • Collaborate with the Site Care Partner to ensure reliable site delivery • Support and train investigators and site staff on protocol requirements, compliance, patient safety, and study risks • Identify operational, quality, and protocol-related issues at an early stage and coordinate their resolution • Agree on appropriate corrective and preventive actions • Complete and follow up on documentation in a timely manner, including the Trial Master File, monitoring reports, follow-up letters, protocol deviations, recruitment progress, and study metrics • Monitor the proper handling of the investigational product • Support database lock activities • Collaborate with internal study teams, service providers, and external clinical trial sites in an international matrix environment

🎯 Requirements

• University degree in life sciences or a comparable vocational qualification, such as nursing, pharmacy, or a medical discipline • At least one year of relevant experience in clinical trial monitoring and clinical site management • Knowledge of clinical trial methodologies, ICH/GCP requirements, and applicable local regulatory requirements • Excellent written and spoken German and English • Ability to assess complex information and data, communicate findings clearly, and derive risk mitigation actions • Strong communication and collaboration skills in a cross-functional matrix environment • Willingness to travel 60–80% within the assigned territory; international travel and occasional weekend travel may be required • Valid driver's license and passport • Preferred: Experience with global clinical trials • Preferred: Therapeutic experience in oncology, vaccines, internal medicine, or infectious diseases

🏖️ Benefits

• Equal treatment and equal opportunities throughout the application process • Reasonable accommodations for applicants and employees with disabilities • Support with applications, the recruitment process, and interviews related to accessibility • Opportunities to contribute and further develop skills and knowledge • A career at Pfizer